CH,Cl, Brz. H20

Q: Predict the major product for the reaction shown. excess CI CH,CH2CI 1. KMnOд/NaOH/н-0 AICI3 AICI3…

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Q: 3.3 Explain the reasons why the reactions provided below DO NOT work and show the other expected…

A: Reasons: a.  The initial reaction will not work because nitrogen of aniline will react fast with…

Q: D. CH,CH;CH,CH, + O +02

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Q: For the reaction shown below, select the expected major product. Br 1. excess NaNH2 2. H20 Br NH2…

A: The reaction given is,

Q: Predict the product of the following reaction. 1. CH3I(x's)/Ag20,heat 2.KMN04, cold, neutral NH2 HO…

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Q: Но a) HO Br ? H20 404150 b) CH3CH2Br CN с) CH3CH,CI H20 ?

A: In reaction a, first the OH- will take proton from the OH group of reactant as it is acidic H.

Q: 1. NANH2 2. CH3Br 3. Na, NH3 NazCr207 H20, H2SO4 4. ВНз 5. HОг, NaOH

A: Welcome to bartleby!

Q: a) Br HO HO ? H20 04150 b) CH3CH2Br CN ? c) CH3CH2CI H20 ?

A: Answer:

Q: 0. Which two structures ionize with loss of bromide to form the same carbocation? Br Br Br 20 Br I…

A: In a chemical reaction; the substance which involves in conversion is said to be reactant whereas…

Q: Predict the following products: 1. BH/THF 2. HO", H,O2, H20 1. О, -78C 2. Zn, CH;CO2H m-CРBА NO2…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Give the major product for the reaction below. A HBr H2 F Ni KMNO4, OH, heat > B H* KMNO4 Br2 cold,…

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Q: a. NaH, THF он b. 60 °C Br

A: Primary alcohol has a carbon bonded -OH group to another carbon bonding. Sodium hydride is a strong…

Q: 1) KMNO4 2) SOCI, 3) H,N- EtzN excess reagents on all steps

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Q: MC02 How many of the compounds shown are not expected to be converted into Grignard reagent on…

A: How many of the compounds shown are not expected to be converted into Grignard reagent on reaction…

Q: Provide a reasonable mechanism for the following reaction. + NH xs. MeBr 样 Br

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Q: (CH3)3C–H 91 (СH3)3C-Br 65 Br-Br 46 Н-Br 88 CH3-Br 70 (B) Draw all monochlorination products…

A: Bond dissociation energy is given by difference of bond energy of reactant and bond energy of…

Q: Predict the major product of the reaction K½Cr,O7 HO, H2SO4

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Q: 2. For the following Alkylhalide indicate which position will react under SN1 reaction conditions…

A: The nucleophilic substitution reaction involves the replacement of one group by other group and it…

Q: II. Predict the products of the ff: elimination reactions and show the mechanisms involve. (a) HO…

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Q: (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is…

A: Ans

Q: Consider the following reactions below: ... Mg ether 1. ether CH, 2. H30 Br IV Compound IV will most…

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Q: Which synthetic route represents the best method for generating the target molecule below? Route A…

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Q: Complete the reaction s by giving the missing product (s) Show the stere0chemistry of the product…

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Q: Predict the product for the following reaction. CH;OH/ H2SO4 OCH, ** OCH OCH3 OH OCH3

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Q: 4. Predict the products: ин от + ін гоём 2 + f ян д дн - - он он - он он

A: The answer to the following question is-

Q: Predict the major product. HNO, H,SO, NO2 NO2 ZON NO2 D C A O O O

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Q: HBr (aecess) b) Br Br Br Br Br Br Br

A: a) Alkynes react with excess HBr producing alkyl halides via carbocation formation mechanism.

Q: Which of these bromides would be best for an SN2 reaction? Br Br CH3 H.C. Br A O A O D OB C.

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: 69 68 diene dienophile 68. A. В. D. none of these 69. А. D. none of these В. Zn/Cu 70 ether + CH212…

A: The first reaction is diels-alder reaction. The second reaction goes through a carbene type…

Q: What are the missing reagents and compounds below ´Na `OH → B Br H,SO, E D OTMS `OH он HO TMS =…

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Q: 1. t-BUOK,t-BUOH CI 2. HBr Br

A: Tertiary butoxide is a hindered base which on reaction with alkyl halide undergo elimination…

Q: 5. Provide reasonable mechanisms for the conversions below. -CH3 NaOH `CH3 H,O Br

A: Detail mechanistic pathway is given below

Q: Predict the product for the following SN1 reaction. Nal II IV 0000

A: The reaction taking place is given as,

Q: a) Br HO но ? H20 04150 b) CH3CH,Br CN c) CH3CH,CI H20 ?

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Q: Find the product OCH, H,N. [H] H,N

A: Detail mechanistic pathway is given below by which we get the final product.

Q: (CHs)2 Cuhi 2. Amel CHSOH,H30* d. Hq SO4 He 504(09) 2.NHOH Br 4) 1a.LATH b. H30 2. (CHs), NH 2.exces…

A: We have to complete the following reactions in sequential order and also have to show intermediate…

Q: 9) Predict the reactants for the ff products: SH (a) CH3OCH2CH2CH3 (b) „OCH3 (c) (d) CH3…

A: the reactants are as follows:

Q: a) Br KOH, etanol CH,l, ZnCu Br b) Bry, H,0 B

A: The answer along with explanation is provided in picture below

Q: Rank these alkyl halides by their SN 2 reaction rate. Br CI Br Br A D

A: SN2 Reactions occured in single step, leaving Nucleophile and attacking of Nucleophile takesplace…

Q: Give the product of the following reaction. HO Br2, FeBr3 а. но, Br + HBr b. но, + HBr Br C. но, Br…

A: Given reaction is bromination of phenol.

Q: 2. Rate these in order of reactivity to S,1 reactions. (1=most reactive) CI CI

A: Answer  The rate of the SN1 reaction depends on stability of carbocation. The stable carbocation…

Q: 6) Which of the following steps would successfully complete the following reaction? OCH3 но. Br2, 2)…

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Q: excess HBr Br Br

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Q: 1. What is the expected major product of the following reactions? Br2 а. FeBr3 Br- AICI3 CI с. AICI3…

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Q: Predict the product for the following Sy1 reaction. Br O Na он II III IV

A: In SN1 reaction, the leaving group in the electrophile leaves first forming a carbocation. Now the…

Q: 8-) following reactions. Predict the major and minor products of the EtO CH,CH,CHCH, L'BuO Br

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Q: 8) Draw the product of the Sn2 reaction illustrated below. Comment on the stereochemistry of the…

A: 8. Given reaction,

Q: 10. Complete the following reactions: , CH3 + KOH - Bm b) CH3 CH2 CH=CHz + Hz0

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